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Volumn 20, Issue 12, 2012, Pages 1265-1269

Variants in the 3′UTR of SNCA do not affect miRNA-433 binding and alpha-synuclein expression

Author keywords

30UTR; expression; miRNA 433; Parkinson's disease; SNCA

Indexed keywords

ALPHA SYNUCLEIN; MESSENGER RNA; MICRORNA; MICRORNA 433; UNCLASSIFIED DRUG; MIRN433 MICRORNA, HUMAN; SNCA PROTEIN, HUMAN;

EID: 84869228626     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2012.84     Document Type: Article
Times cited : (17)

References (20)
  • 4
    • 33645111633 scopus 로고    scopus 로고
    • Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease
    • Mizuta I, Satake W, Nakabayashi Y et al: Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease. Hum Mol Genet 2006; 15: 1151-1158.
    • (2006) Hum Mol Genet , vol.15 , pp. 1151-1158
    • Mizuta, I.1    Satake, W.2    Nakabayashi, Y.3
  • 5
    • 70549084415 scopus 로고    scopus 로고
    • Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
    • Satake W, Nakabayashi Y, Mizuta I et al: Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet 2009; 41: 1303-1307.
    • (2009) Nat Genet , vol.41 , pp. 1303-1307
    • Satake, W.1    Nakabayashi, Y.2    Mizuta, I.3
  • 6
    • 70549088602 scopus 로고    scopus 로고
    • Genome-wide association study reveals genetic risk underlying Parkinson's disease
    • Simon-Sanchez J, Schulte C, Bras JM et al: Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 2009; 41: 1308-1312.
    • (2009) Nat Genet , vol.41 , pp. 1308-1312
    • Simon-Sanchez, J.1    Schulte, C.2    Bras, J.M.3
  • 8
    • 77951249562 scopus 로고    scopus 로고
    • Post-transcriptional regulation of alpha-synuclein expression by mir-7 and mir-153
    • Doxakis E: Post-transcriptional regulation of alpha-synuclein expression by mir-7 and mir-153. J Biol Chem 2010; 285: 12726-12734.
    • (2010) J Biol Chem , vol.285 , pp. 12726-12734
    • Doxakis, E.1
  • 10
    • 0027337422 scopus 로고
    • Parkinson's Disease Society Brain Bank, London: Overview and research
    • Daniel SE, Lees AJ: Parkinson's Disease Society Brain Bank, London: overview and research. J Neural Transm Suppl, 1993; 39: 165-172. (Pubitemid 23216938)
    • (1993) Journal of Neural Transmission, Supplement , Issue.39 , pp. 165-172
    • Daniel, S.E.1    Lees, A.J.2
  • 11
    • 0000937686 scopus 로고
    • Tests for linear trends in proportions and frequencies
    • Armitage P: Tests for linear trends in proportions and frequencies. Biometrics 1955; 11: 375-386.
    • (1955) Biometrics , vol.11 , pp. 375-386
    • Armitage, P.1
  • 13
    • 63749085796 scopus 로고    scopus 로고
    • A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats
    • Chung BD, Kayserili H, Ai M et al: A mutation in the signal sequence of LRP5 in a family with an osteoporosis-pseudoglioma syndrome (OPPG)-like phenotype indicates a novel disease mechanism for trinucleotide repeats. Hum Mutat 2009; 30: 641-648.
    • (2009) Hum Mutat , vol.30 , pp. 641-648
    • Chung, B.D.1    Kayserili, H.2    Ai, M.3
  • 15
    • 84863860992 scopus 로고    scopus 로고
    • A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease
    • e-pub ahead of print 11 November 2011 doi:10.1007/s12031-011-9669-1
    • Cardo LF, Coto E, de Mena L et al: A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease. J Mol Neurosci 2011; e-pub ahead of print 11 November 2011; doi:10.1007/s12031-011-9669-1.
    • (2011) J Mol Neurosci
    • Cardo, L.F.1    Coto, E.2    De Mena, L.3
  • 16
    • 40749145370 scopus 로고    scopus 로고
    • Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein
    • Wang G, van der Walt JM, Mayhew G et al: Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein. Am J Hum Genet 2008; 82: 283-289.
    • (2008) Am J Hum Genet , vol.82 , pp. 283-289
    • Wang, G.1    Van Der Walt, J.M.2    Mayhew, G.3
  • 17
    • 42549095759 scopus 로고    scopus 로고
    • Elevated alpha-synuclein mRNA levels in individual UV-laser- microdissected dopaminergic substantia nigra neurons in idiopathic Parkinson's disease
    • Grundemann J, Schlaudraff F, Haeckel O, Liss B: Elevated alpha-synuclein mRNA levels in individual UV-laser-microdissected dopaminergic substantia nigra neurons in idiopathic Parkinson's disease. Nucleic Acids Res 2008; 36: e38.
    • (2008) Nucleic Acids Res , vol.36
    • Grundemann, J.1    Schlaudraff, F.2    Haeckel, O.3    Liss, B.4
  • 18
    • 35848966980 scopus 로고    scopus 로고
    • Alpha-Synuclein and Parkinson disease susceptibility
    • Winkler S, Hagenah J, Lincoln S et al: Alpha-Synuclein and Parkinson disease susceptibility. Neurology 2007; 69: 1745-1750.
    • (2007) Neurology , vol.69 , pp. 1745-1750
    • Winkler, S.1    Hagenah, J.2    Lincoln, S.3
  • 19
    • 84878770329 scopus 로고    scopus 로고
    • Wellcome Trust Case Control Consortium 2(WTCCC2): A two-stage meta-analysis identifies several new loci for Parkinson's disease
    • International Parkinson's Disease Genomics Consortium (IPDGC)
    • International Parkinson's Disease Genomics Consortium (IPDGC); Wellcome Trust Case Control Consortium 2(WTCCC2): A two-stage meta-analysis identifies several new loci for Parkinson's disease. PLoS Genet 2011; 7: e1002142.
    • (2011) PLoS Genet , vol.7
  • 20
    • 78650550275 scopus 로고    scopus 로고
    • Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21
    • Spencer CC, Plagnol V, Strange A et al: Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Hum Mol Genet 2011; 20: 345-353.
    • (2011) Hum Mol Genet , vol.20 , pp. 345-353
    • Spencer, C.C.1    Plagnol, V.2    Strange, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.